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David Piñeyro
Researcher at Catalan Institution for Research and Advanced Studies
Publications - 29
Citations - 855
David Piñeyro is an academic researcher from Catalan Institution for Research and Advanced Studies. The author has contributed to research in topics: Epigenetics & Transfer RNA. The author has an hindex of 12, co-authored 25 publications receiving 527 citations. Previous affiliations of David Piñeyro include Spanish National Research Council.
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Journal ArticleDOI
Epigenetic prediction of response to anti-PD-1 treatment in non-small-cell lung cancer: a multicentre, retrospective analysis.
Michael Duruisseaux,Anna Martínez-Cardús,Maria E. Calleja-Cervantes,Sebastian Moran,Manuel Castro de Moura,Veronica Davalos,David Piñeyro,Montse Sanchez-Cespedes,Nicolas Girard,Marie Brevet,Etienne Giroux-Leprieur,Coraline Dumenil,Monica Pradotto,Paolo Bironzo,Enrica Capelletto,Silvia Novello,Alexis B. Cortot,Marie-Christine Copin,Niki Karachaliou,Maria Gonzalez-Cao,Sergio Peralta,Luis M. Montuenga,Ignacio Gil-Bazo,Iosune Baraibar,Maria D. Lozano,Mar Varela,Jose Carlos Ruffinelli,Ramon Palmero,Ernest Nadal,Teresa Moran,Lidia Perez,Immaculada Ramos,Qingyang Xiao,Agustín F. Fernández,Mario F. Fraga,Marta Gut,Ivo Gut,Cristina Teixidó,Noelia Vilariño,Aleix Prat,Noemi Reguart,Amparo Benito,Pilar Garrido,Isabel Barragan,Isabel Barragan,Jean-François Emile,Rafael Rosell,Elisabeth Brambilla,Manel Esteller +48 more
TL;DR: The epigenetic milieu of NSCLC tumours indicates which patients are most likely to benefit from nivolumab or pembrolizumab treatments, and the methylation status of FOXP1 could be associated with validated predictive biomarkers such as PD-L1 staining and mutational load to better select patients who will experience clinical benefit with PD-1 blockade.
Journal ArticleDOI
A-to-I editing on tRNAs: biochemical, biological and evolutionary implications.
Adrian Gabriel Torres,David Piñeyro,Liudmila Filonava,Travis H. Stracker,Eduard Batlle,Lluís Ribas de Pouplana +5 more
TL;DR: Current understanding on the role of inosine in tRNAs, the enzymes that catalyze the modification and the evolutionary link between such enzymes and other deaminases are reviewed.
Journal ArticleDOI
Epigenetic loss of RNA-methyltransferase NSUN5 in glioma targets ribosomes to drive a stress adaptive translational program
Maxime Janin,Vanessa Ortiz-Barahona,Manuel Castro de Moura,Anna Martínez-Cardús,Pere Llinàs-Arias,Marta Soler,Daphna Nachmani,Joffrey Pelletier,Ulrike Schumann,Maria E. Calleja-Cervantes,Sebastian Moran,Sonia Guil,Alberto Bueno-Costa,David Piñeyro,Montserrat Pérez-Salvia,Margalida Rosselló-Tortella,Laia Piqué,Joan Josep Bech-Serra,Carolina De La Torre,August Vidal,María Martínez-Iniesta,Juan F. Martín-Tejera,Alberto Villanueva,Alexandra Arias,Isabel Cuartas,Ana M. Aransay,Andres Morales La Madrid,Angel M. Carcaboso,Vicente Santa-Maria,Jaume Mora,Agustín F. Fernández,Mario F. Fraga,Iban Aldecoa,Leire Pedrosa,Francesc Graus,Noemi Vidal,Fina Martínez-Soler,Avelina Tortosa,Cristina Carrato,C. Balana,Matthew W. Boudreau,Paul J. Hergenrother,Peter Kötter,K. D. Entian,Jürgen Hench,Stephan Frank,Sheila Mansouri,Gelareh Zadeh,Pablo D. Dans,Modesto Orozco,George Thomas,George Thomas,Sandra Blanco,Joan Seoane,Joan Seoane,Thomas Preiss,Thomas Preiss,Pier Paolo Pandolfi,Manel Esteller +58 more
TL;DR: It is found that human glioma cells undergo DNA methylation-associated epigenetic silencing of NSUN5, a candidate RNA methyltransferase for 5-methylcytosine, which exhibits tumor-suppressor characteristics in vivo gliomas models and leads to the emergence of an adaptive translational program for survival under conditions of cellular stress.
Journal ArticleDOI
Inosine modifications in human tRNAs are incorporated at the precursor tRNA level
Adrian Gabriel Torres,David Piñeyro,Marta Rodríguez-Escribà,Noelia Camacho,Oscar Reina,Adélaïde Saint-Léger,Liudmila Filonava,Eduard Batlle,Lluís Ribas de Pouplana +8 more
TL;DR: RNAseq is presented as a powerful tool to study post-transcriptional tRNA modifications at the precursor tRNA level and gives the first insights on the biology of I34 tRNA modification in metazoans.
Journal ArticleDOI
Molecular Features of Cancers Exhibiting Exceptional Responses to Treatment
David A. Wheeler,Naoko Takebe,Toshinori Hinoue,Katherine A. Hoadley,Maria F. Cardenas,Alina M Hamilton,Peter W. Laird,Linghua Wang,Adrienne Johnson,Ninad Dewal,Vincent A. Miller,David Piñeyro,Manuel Castro de Moura,Manel Esteller,Hui Shen,Jean C. Zenklusen,Roy Tarnuzzer,Lisa M. McShane,James V. Tricoli,Paul Williams,Irina A. Lubensky,Geraldine O'Sullivan-Coyne,Elise C. Kohn,Richard F. Little,Jeffrey White,Shakun Malik,Lyndsay Harris,Carol J. Weil,Alice P. Chen,Chris Karlovich,Brian Rodgers,Lalitha K. Shankar,Paula M. Jacobs,Tracy S. Nolan,Jianhong Hu,Donna M. Muzny,Harshavardhan Doddapaneni,Viktoriya Korchina,Julie M. Gastier-Foster,Jay Bowen,Kristen M. Leraas,Elijah F. Edmondson,James H. Doroshow,Barbara A. Conley,S. Percy Ivy,Louis M. Staudt +45 more
TL;DR: Analysis of tumor biopsies from an unbiased cohort of 111 exceptional responder patients revealed synthetic lethal relationships that may be exploited therapeutically and rare genetic lesions that favor therapeutic success, while also providing a wealth of testable hypotheses regarding oncogenic mechanisms that may influence the response to cancer therapy.